(Q52127817)

22 April 2018

title

Congenital renal dysplasia, retinal dysplasia and mental retardation associated with hyperprolinuria and hyper-oh-prolinuria (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5706039

21 June 2023

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5706039

21 June 2023

author name string

T. Rokkones

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5706039

21 June 2023

A. C. Loken

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5706039

21 June 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5706039

21 June 2023

publication date

1 May 1968

1 reference

22 April 2018

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1651-2227.1968.tb04682.x

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1968.tb04682.x/fullpdf

21 June 2023

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

Acta Paediatrica Scandinavica

21 June 2023

published in

1 reference

22 April 2018

volume

57

1 reference

22 April 2018

issue

3

1 reference

22 April 2018

page(s)

225-229

1 reference

22 April 2018

Hereditary renal dysplasia and blindness

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.

21 June 2023

2

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

Familial dysplasia of kidneys, liver and pancreas: a probably genetically determined syndrome.

21 June 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS

21 June 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

The persistence of foetal structures in pyelonephritic kidneys

21 June 2023

7

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

Congenital hereditary hematuria

21 June 2023

12

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

Familial Hyperprolinemia, Cerebral Dysfunction and Renal Anomalies Occurring in a Family with Hereditary Nephropathy and Deafness

21 June 2023

13

1 reference

https://api.crossref.org/works/10.1111/J.1651-2227.1968.TB04682.X

21 June 2023

Identifiers

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jwdyok6bwbdc3nldhpwdgjgw6q

mapped directly with Wikidata item

30 July 2022

based on heuristic

Fatcat ID

release_jwdyok6bwbdc3nldhpwdgjgw6q

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jwdyok6bwbdc3nldhpwdgjgw6q

mapped directly with Wikidata item

30 July 2022

based on heuristic

https://api.fatcat.wiki/v0/release/jwdyok6bwbdc3nldhpwdgjgw6q

1 reference